Canonical Allele Identifier: CA2244455746
Gene: ALOX15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631909_4631918delinsCCAGCTGCCA , CM000679.2:g.4631909_4631918delinsCCAGCTGCCA GRCh38
NC_000017.10:g.4535204_4535213delinsCCAGCTGCCA , CM000679.1:g.4535204_4535213delinsCCAGCTGCCA GRCh37
NC_000017.9:g.4481953_4481962delinsCCAGCTGCCA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1780_1789delinsTGGCAGCTGG MANE Select ENSP00000293761.3:p.Trp594=
ENST00000570836.6:c.1780_1789delinsTGGCAGCTGG ENSP00000458832.1:p.Trp594=
ENST00000293761.7:c.1780_1789delinsTGGCAGCTGG ENSP00000293761.3:p.Trp594=
ENST00000570836.5:c.1780_1789delinsTGGCAGCTGG ENSP00000458832.1:p.Trp594=
ENST00000574640.1:c.1663_1672delinsTGGCAGCTGG ENSP00000460483.1:p.Trp555=
NM_001140.3:c.1780_1789delinsTGGCAGCTGG NP_001131.3:p.Trp594=
NM_001140.4:c.1780_1789delinsTGGCAGCTGG NP_001131.3:p.Trp594=
NM_001140.5:c.1780_1789delinsTGGCAGCTGG MANE Select NP_001131.3:p.Trp594=
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